Mutagenetix > Incidental Mutation

Incidental Mutation 'R1672:Apobr'

187703

Institutional Source

Beutler Lab

Gene Symbol

Apobr

Ensembl Gene

ENSMUSG00000042759

Gene Name

apolipoprotein B receptor

Synonyms

Apob48r, Apob-48r

MMRRC Submission

039708-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.089) question?

Stock #

R1672 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

126184114-126188284 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 126186723 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glycine at position 745 (R745G)

Ref Sequence

ENSEMBL: ENSMUSP00000042028 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000032962] [ENSMUST00000039522] [ENSMUST00000058429] [ENSMUST00000084589] [ENSMUST00000098036] [ENSMUST00000116269] [ENSMUST00000125508] [ENSMUST00000131860] [ENSMUST00000138558] [ENSMUST00000137646] [ENSMUST00000144173] [ENSMUST00000150917] [ENSMUST00000147086] [ENSMUST00000150311] [ENSMUST00000128970] [ENSMUST00000150587]

AlphaFold

Q8VBT6

Predicted Effect

probably benign
Transcript: ENSMUST00000032962

SMART Domains

Protein: ENSMUSP00000032962
Gene: ENSMUSG00000030720

Domain	Start	End	E-Value	Type
Pfam:CLN3	37	438	3.5e-215	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000039522
AA Change: R745G

PolyPhen 2 Score 0.314 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000042028
Gene: ENSMUSG00000042759
AA Change: R745G

Domain	Start	End	E-Value	Type
low complexity region	45	59	N/A	INTRINSIC
low complexity region	171	181	N/A	INTRINSIC
low complexity region	351	363	N/A	INTRINSIC
low complexity region	381	396	N/A	INTRINSIC
low complexity region	465	476	N/A	INTRINSIC
low complexity region	588	608	N/A	INTRINSIC
low complexity region	837	862	N/A	INTRINSIC
low complexity region	869	881	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000058429

SMART Domains

Protein: ENSMUSP00000054637
Gene: ENSMUSG00000044701

Domain	Start	End	E-Value	Type
signal peptide	1	28	N/A	INTRINSIC
low complexity region	137	148	N/A	INTRINSIC
low complexity region	160	177	N/A	INTRINSIC
low complexity region	210	228	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000084589

SMART Domains

Protein: ENSMUSP00000081636
Gene: ENSMUSG00000030720

Domain	Start	End	E-Value	Type
Pfam:CLN3	37	438	3.5e-215	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000098036

SMART Domains

Protein: ENSMUSP00000095644
Gene: ENSMUSG00000030720

Domain	Start	End	E-Value	Type
Pfam:CLN3	37	414	4.3e-191	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000116269

SMART Domains

Protein: ENSMUSP00000111973
Gene: ENSMUSG00000030720

Domain	Start	End	E-Value	Type
Pfam:CLN3	39	437	1.6e-140	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000125508

SMART Domains

Protein: ENSMUSP00000117561
Gene: ENSMUSG00000030720

Domain	Start	End	E-Value	Type
Pfam:CLN3	37	76	1.2e-17	PFAM
Pfam:CLN3	73	151	2.8e-38	PFAM

Predicted Effect

silent
Transcript: ENSMUST00000131860

Predicted Effect

probably benign
Transcript: ENSMUST00000138558

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000134406

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000128049

Predicted Effect

probably benign
Transcript: ENSMUST00000137646

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000128225

Predicted Effect

probably benign
Transcript: ENSMUST00000144173

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000134246

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000134498

Predicted Effect

probably benign
Transcript: ENSMUST00000150917

SMART Domains

Protein: ENSMUSP00000138688
Gene: ENSMUSG00000030720

Domain	Start	End	E-Value	Type
Pfam:CLN3	37	77	1.6e-18	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000147086

Predicted Effect

probably benign
Transcript: ENSMUST00000150311

SMART Domains

Protein: ENSMUSP00000116160
Gene: ENSMUSG00000030720

Domain	Start	End	E-Value	Type
Pfam:CLN3	37	69	1.5e-14	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000128970

SMART Domains

Protein: ENSMUSP00000114901
Gene: ENSMUSG00000030720

Domain	Start	End	E-Value	Type
Pfam:CLN3	37	196	1.2e-87	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000150587

SMART Domains

Protein: ENSMUSP00000118054
Gene: ENSMUSG00000030720

Domain	Start	End	E-Value	Type
Pfam:CLN3	37	70	4.1e-15	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153790

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.4%
20x: 92.7%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Apolipoprotein B48 receptor is a macrophage receptor that binds to the apolipoprotein B48 of dietary triglyceride (TG)-rich lipoproteins. This receptor may provide essential lipids, lipid-soluble vitamins and other nutrients to reticuloendothelial cells. If overwhelmed with elevated plasma triglyceride, the apolipoprotein B48 receptor may contribute to foam cell formation, endothelial dysfunction, and atherothrombogenesis. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 103 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310079G19Rik	G	A	16: 88,424,096 (GRCm39)	Q132*	probably null	Het
Aadacl4	T	A	4: 144,349,889 (GRCm39)	L382*	probably null	Het
Afg3l2	A	G	18: 67,540,493 (GRCm39)	I672T	probably benign	Het
Aftph	A	T	11: 20,676,762 (GRCm39)	D282E	probably benign	Het
Agpat5	A	G	8: 18,920,930 (GRCm39)	N161S	probably benign	Het
Alpk2	C	T	18: 65,414,030 (GRCm39)	E1562K	probably damaging	Het
Anxa2	TCCC	TCC	9: 69,397,036 (GRCm39)		probably null	Het
Arrdc5	T	C	17: 56,607,144 (GRCm39)	T34A	possibly damaging	Het
Astl	T	C	2: 127,189,163 (GRCm39)	L163P	probably damaging	Het
Atf7ip2	A	T	16: 10,027,005 (GRCm39)	H91L	probably damaging	Het
Atp13a3	A	T	16: 30,151,092 (GRCm39)	S1073T	possibly damaging	Het
Bcl2a1a	A	T	9: 88,839,503 (GRCm39)	I134L	probably damaging	Het
Brinp1	T	C	4: 68,747,520 (GRCm39)		probably null	Het
Capn9	A	G	8: 125,340,570 (GRCm39)	N578S	probably benign	Het
Casp2	T	A	6: 42,245,842 (GRCm39)	D166E	probably damaging	Het
Ccr1l1	A	T	9: 123,777,544 (GRCm39)	I301N	probably damaging	Het
Chtop	T	A	3: 90,414,874 (GRCm39)	T15S	probably damaging	Het
Coq5	T	A	5: 115,417,975 (GRCm39)		probably null	Het
Crbn	G	A	6: 106,772,886 (GRCm39)	P34L	probably damaging	Het
Crisp1	G	T	17: 40,619,760 (GRCm39)	D59E	possibly damaging	Het
Cyp4f14	A	T	17: 33,128,210 (GRCm39)	D268E	probably benign	Het
D5Ertd579e	T	C	5: 36,770,621 (GRCm39)	D1258G	possibly damaging	Het
Dcp1b	T	C	6: 119,194,872 (GRCm39)	S531P	probably benign	Het
Defb25	T	C	2: 152,464,410 (GRCm39)	M45V	probably benign	Het
Dffa	T	C	4: 149,190,702 (GRCm39)	L77P	probably damaging	Het
Dixdc1	T	C	9: 50,601,164 (GRCm39)	Q361R	probably damaging	Het
Dnah1	A	G	14: 30,998,157 (GRCm39)	L2560P	probably damaging	Het
Fabp5	A	G	3: 10,080,601 (GRCm39)	T108A	probably benign	Het
Fam149a	T	G	8: 45,792,411 (GRCm39)		probably null	Het
Fam20c	A	G	5: 138,793,056 (GRCm39)	Y430C	probably damaging	Het
Fat1	A	G	8: 45,489,872 (GRCm39)	T3595A	probably damaging	Het
Fbp1	A	G	13: 63,015,245 (GRCm39)	Y245H	probably damaging	Het
Frem1	C	T	4: 82,917,128 (GRCm39)	R605H	probably benign	Het
Fscb	A	G	12: 64,518,292 (GRCm39)	I1058T	unknown	Het
Fyb2	A	G	4: 104,808,059 (GRCm39)	K373R	probably benign	Het
Ggta1	A	T	2: 35,292,145 (GRCm39)	Y387*	probably null	Het
Gm18856	T	C	13: 14,140,342 (GRCm39)		probably benign	Het
Gm572	T	C	4: 148,752,966 (GRCm39)	S282P	possibly damaging	Het
Gpd2	A	T	2: 57,247,712 (GRCm39)	I552F	probably damaging	Het
Grk5	T	C	19: 61,074,653 (GRCm39)		probably null	Het
Hivep1	T	C	13: 42,313,760 (GRCm39)	V2000A	probably damaging	Het
Ipo5	C	T	14: 121,170,714 (GRCm39)	L466F	probably damaging	Het
Itgb1	G	A	8: 129,458,526 (GRCm39)	S785N	probably damaging	Het
Itpr3	G	A	17: 27,307,987 (GRCm39)	R258K	probably benign	Het
Kcnk12	A	G	17: 88,053,747 (GRCm39)	V305A	probably benign	Het
Klf5	C	T	14: 99,538,986 (GRCm39)	T133I	probably damaging	Het
Lrig2	A	G	3: 104,399,128 (GRCm39)	I178T	probably damaging	Het
Lyrm4	A	T	13: 36,276,907 (GRCm39)	M30K	probably benign	Het
Mpv17	A	G	5: 31,311,063 (GRCm39)	Y7H	probably damaging	Het
Mrps22	T	C	9: 98,478,869 (GRCm39)		probably null	Het
Myof	A	T	19: 37,931,927 (GRCm39)	W967R	probably damaging	Het
Naip1	C	T	13: 100,559,657 (GRCm39)	D1116N	probably benign	Het
Or1e33	T	C	11: 73,738,781 (GRCm39)	T57A	probably benign	Het
Or6c66b	C	A	10: 129,376,561 (GRCm39)	H52N	probably benign	Het
Or8g50	G	A	9: 39,648,492 (GRCm39)	C127Y	probably damaging	Het
Or9k2b	T	C	10: 130,016,261 (GRCm39)	T163A	probably benign	Het
Ovol2	T	C	2: 144,147,710 (GRCm39)	Y180C	probably damaging	Het
Pacs1	T	C	19: 5,202,337 (GRCm39)	S418G	probably benign	Het
Pcdh1	T	C	18: 38,325,233 (GRCm39)	E903G	probably damaging	Het
Pcdhb15	A	T	18: 37,607,713 (GRCm39)	Y315F	probably damaging	Het
Pex1	T	C	5: 3,676,085 (GRCm39)	L891P	probably damaging	Het
Potefam1	T	A	2: 111,051,119 (GRCm39)	M226L	probably benign	Het
Ppfia2	G	A	10: 106,666,429 (GRCm39)	M378I	possibly damaging	Het
Ppp1r9a	T	A	6: 5,143,491 (GRCm39)		probably null	Het
Prm3	T	C	16: 10,608,563 (GRCm39)	E64G	possibly damaging	Het
Prmt6	T	C	3: 110,157,887 (GRCm39)	D134G	possibly damaging	Het
Prss42	G	A	9: 110,629,996 (GRCm39)	G250D	probably damaging	Het
Pwwp2b	G	A	7: 138,834,747 (GRCm39)	V63I	probably benign	Het
Rbm17	T	C	2: 11,590,530 (GRCm39)	D375G	possibly damaging	Het
Rhbdl1	A	T	17: 26,055,383 (GRCm39)		probably null	Het
Rims2	T	A	15: 39,155,584 (GRCm39)	D128E	probably benign	Het
Rock2	A	G	12: 17,015,653 (GRCm39)	K850R	probably benign	Het
Rreb1	T	C	13: 38,114,513 (GRCm39)	I624T	probably benign	Het
Rrp36	A	T	17: 46,983,340 (GRCm39)	D91E	probably damaging	Het
Scn7a	C	T	2: 66,527,944 (GRCm39)	D849N	possibly damaging	Het
Sec24a	A	T	11: 51,634,775 (GRCm39)	Y50*	probably null	Het
Sh2d4b	A	G	14: 40,614,921 (GRCm39)	M1T	probably null	Het
Slc4a7	A	G	14: 14,760,247 (GRCm38)	I561V	possibly damaging	Het
Slc7a12	T	C	3: 14,564,337 (GRCm39)	V70A	possibly damaging	Het
Slfnl1	A	T	4: 120,392,972 (GRCm39)	I355F	probably damaging	Het
Spata2	C	T	2: 167,325,439 (GRCm39)	R460H	probably damaging	Het
Stk11ip	C	T	1: 75,505,629 (GRCm39)	Q433*	probably null	Het
Susd1	T	C	4: 59,411,395 (GRCm39)	Y146C	probably damaging	Het
Susd5	A	T	9: 113,897,890 (GRCm39)	D115V	probably damaging	Het
Tas2r110	T	A	6: 132,845,029 (GRCm39)	V20E	probably damaging	Het
Tbc1d4	T	C	14: 101,712,651 (GRCm39)	Y694C	possibly damaging	Het
Tmem131	T	C	1: 36,863,840 (GRCm39)	E640G	probably damaging	Het
Togaram1	A	G	12: 65,068,342 (GRCm39)	T1782A	probably benign	Het
Trim24	T	C	6: 37,892,214 (GRCm39)	L249P	probably damaging	Het
Ttf1	T	C	2: 28,957,164 (GRCm39)	I478T	probably damaging	Het
Upf2	T	A	2: 6,044,908 (GRCm39)		probably null	Het
Urb1	A	T	16: 90,584,285 (GRCm39)	C566S	probably damaging	Het
Vmn1r191	T	C	13: 22,363,262 (GRCm39)	N164S	probably benign	Het
Vmn2r81	T	A	10: 79,104,112 (GRCm39)	V245E	probably damaging	Het
Vwce	T	A	19: 10,630,459 (GRCm39)	F506Y	possibly damaging	Het
Wnt8b	T	C	19: 44,499,715 (GRCm39)	F155L	probably damaging	Het
Xrra1	A	T	7: 99,547,647 (GRCm39)	I279F	probably benign	Het
Zfp229	T	C	17: 21,964,828 (GRCm39)	S353P	probably damaging	Het
Zfp607b	C	T	7: 27,391,948 (GRCm39)	H8Y	possibly damaging	Het
Zfp933	A	T	4: 147,910,476 (GRCm39)	H373Q	probably damaging	Het
Zfp938	A	G	10: 82,060,982 (GRCm39)	L546P	probably benign	Het
Zfp988	C	T	4: 147,415,739 (GRCm39)	R58C	probably benign	Het
Zkscan14	C	T	5: 145,138,464 (GRCm39)	V8I	probably benign	Het

Other mutations in Apobr

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01812:Apobr	APN	7	126,187,094 (GRCm39)	missense	probably damaging	1.00
IGL02373:Apobr	APN	7	126,184,563 (GRCm39)	missense	probably damaging	1.00
IGL02383:Apobr	APN	7	126,185,779 (GRCm39)	missense	probably benign	0.35
R0626:Apobr	UTSW	7	126,185,827 (GRCm39)	missense	possibly damaging	0.73
R1142:Apobr	UTSW	7	126,186,654 (GRCm39)	missense	probably benign	0.01
R1711:Apobr	UTSW	7	126,184,151 (GRCm39)	start gained	probably null
R1865:Apobr	UTSW	7	126,185,140 (GRCm39)	missense	probably benign	0.00
R1971:Apobr	UTSW	7	126,185,397 (GRCm39)	missense	probably benign	0.00
R1985:Apobr	UTSW	7	126,186,903 (GRCm39)	missense	possibly damaging	0.66
R2130:Apobr	UTSW	7	126,186,378 (GRCm39)	missense	probably benign	0.15
R2143:Apobr	UTSW	7	126,186,288 (GRCm39)	missense	probably benign	0.01
R4497:Apobr	UTSW	7	126,186,694 (GRCm39)	splice site	probably null
R4693:Apobr	UTSW	7	126,186,019 (GRCm39)	missense	probably damaging	0.96
R4797:Apobr	UTSW	7	126,186,756 (GRCm39)	missense	probably benign	0.30
R4814:Apobr	UTSW	7	126,185,859 (GRCm39)	missense	probably benign	0.03
R5000:Apobr	UTSW	7	126,185,729 (GRCm39)	missense	possibly damaging	0.53
R5153:Apobr	UTSW	7	126,186,904 (GRCm39)	missense	possibly damaging	0.92
R5176:Apobr	UTSW	7	126,184,188 (GRCm39)	missense	probably damaging	1.00
R5285:Apobr	UTSW	7	126,184,175 (GRCm39)	unclassified	probably benign
R5296:Apobr	UTSW	7	126,187,196 (GRCm39)	missense	probably damaging	0.96
R5579:Apobr	UTSW	7	126,186,847 (GRCm39)	missense	probably benign	0.00
R9025:Apobr	UTSW	7	126,185,629 (GRCm39)	missense	possibly damaging	0.94
R9063:Apobr	UTSW	7	126,185,920 (GRCm39)	missense	probably benign	0.00
R9245:Apobr	UTSW	7	126,186,507 (GRCm39)	nonsense	probably null
R9405:Apobr	UTSW	7	126,184,704 (GRCm39)	missense	possibly damaging	0.95
R9444:Apobr	UTSW	7	126,185,140 (GRCm39)	missense	probably benign	0.00
R9688:Apobr	UTSW	7	126,186,663 (GRCm39)	missense	probably benign	0.08
Z1088:Apobr	UTSW	7	126,184,203 (GRCm39)	missense	probably benign	0.00
Z1176:Apobr	UTSW	7	126,186,436 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- AGCTTGGGAAAGCCTGGTGTTC -3'
(R):5'- AGGCACAGCTACTGTGGGGATTTG -3'

Sequencing Primer
(F):5'- AAAGCCTGGTGTTCCGAGG -3'
(R):5'- TGGTGTGTCTGCTGCCC -3'

Posted On

2014-05-09